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International Journal of Molecular Sciences|April 13, 2023
New Insight into the Genotype-Phenotype Correlation of PRPH2-Related Diseases Based on a Large Chinese Cohort and Literature ReviewYingwei Wang, Junwen Wang, Yi Jiang, et al.Investigative Ophthalmology & Visual Science|December 11, 2025
Ubap1l Knockout Mice Model Recapitulates Retinal Degeneration Phenotype Observed in Patients and Exhibits Irregular Photoreceptor MorphologyYingwei Wang, Shuhan Zhang, Yuxi Zheng, et al.The British Journal of Ophthalmology|September 30, 2022
Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritanceYingwei Wang, Xueshan Xiao, Xueqing Li, et al.Plos One|November 1, 2011
Is mitochondrial tRNA(phe) variant m.593T>C a synergistically pathogenic mutation in Chinese LHON families with m.11778G>A?A-Mei Zhang, Hans-Jürgen Bandelt, Xiaoyun Jia, et al.Molecular Vision|March 30, 2007
Mutations in NYX of individuals with high myopia, but without night blindnessQingjiong Zhang, Xueshan Xiao, Shiqiang Li, et al.Acta Radiologica (Stockholm, Sweden : 1987)|May 5, 2010
B-type natriuretic peptide for prevention of contrast-induced nephropathy in patients with heart failure undergoing primary percutaneous coronary interventionJing Zhang, Xianghua Fu, Xinwei Jia, et al.Journal of Comparative Effectiveness Research|December 15, 2023
Real-world use of inotuzumab ozogamicin is associated with lower health care costs than blinatumomab in patients with acute lymphoblastic leukemia in the first relapsed/refractory settingAlexander Russell-Smith, Louise Murphy, Amy Nguyen, et al.Plos One|November 24, 2011
Mitochondrial DNA haplogroup background affects LHON, but not suspected LHON, in Chinese patientsA-Mei Zhang, Xiaoyun Jia, Rui Bi, et al.Investigative Ophthalmology & Visual Science|April 25, 2023
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic MechanismYingwei Wang, Wenmin Sun, Xueshan Xiao, et al.Investigative Ophthalmology & Visual Science|May 11, 2013
Comprehensive mutation analysis by whole-exome sequencing in 41 Chinese families with Leber congenital amaurosisYabin Chen, Qingyan Zhang, Tao Shen, et al.Pageof 22